A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009684



Internal ID19098902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:2806780..2925450hg38UCSC Ensembl
Innerchr1:2723345..2842015hg19UCSC Ensembl
Innerchr1:2713205..2831875hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38118671
hg19118671
hg18118671
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12n100
Supporting Variantsnssv3469851, nssv3463686, nssv3474270
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009684
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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